Clinical Research Associate

Are you passionate about making a difference in the world of healthcare? Do you have a strong background in clinical research and a desire to contribute to the development of life-saving treatments? If so, we have an exciting opportunity for you at Novo Nordisk. We are seeking a motivated and experienced Clinical Research Associate to join our team and play a crucial role in advancing our clinical trials. As a member of our team, you will have the chance to work with cutting-edge technology and collaborate with top researchers in the field. If you have a strong attention to detail, excellent organizational skills, and a drive to constantly learn and improve, we encourage you to apply for this position.

1. Conduct clinical research: The primary responsibility of this role is to conduct clinical research, including planning, implementing, and monitoring clinical trials in compliance with regulatory requirements and company protocols.
2. Ensure data accuracy and integrity: The Clinical Research Associate (CRA) is responsible for ensuring the accuracy and integrity of all clinical trial data collected, including data entry, verification, and quality control.
3. Collaborate with research team: The CRA will work closely with cross-functional teams, including researchers, regulatory affairs, and data management, to support the execution of clinical trials and ensure study objectives are met.
4. Monitor and report on trial progress: The CRA will regularly monitor and report on the progress of clinical trials, including identifying and resolving any issues or discrepancies, and providing updates to the research team and management.
5. Maintain regulatory compliance: It is the responsibility of the CRA to maintain regulatory compliance throughout the clinical trial process, including ensuring all documentation and processes adhere to applicable regulations and guidelines.
6. Train and educate study participants: As needed, the CRA will be responsible for training and educating study participants on trial protocols and procedures, as well as collecting informed consent.
7. Maintain trial supplies and equipment: The CRA will be responsible for maintaining and tracking all trial supplies and equipment, ensuring they are properly stored and utilized in accordance with protocols.
8. Continuous learning and improvement: The CRA should have a drive to constantly learn and improve their skills and knowledge in the field of clinical research, staying up-to-date with industry best practices and advancements.
9. Represent the company: The CRA will act as a representative of the company, interacting with study participants, investigators, and vendors in a professional and ethical manner.
10. Adhere to company policies and procedures: The CRA is expected to adhere to all company policies and procedures, including those related to safety, confidentiality, and data protection.

According to JobzMall, the average salary range for a Clinical Research Associate in Princeton, NJ, USA is $68,000 to $96,000 per year. However, this can vary depending on factors such as experience, education, and the specific company or research organization. Some Clinical Research Associates may also receive bonuses or other benefits in addition to their base salary. It is important to note that salary ranges can also vary based on location, with some areas having higher salaries due to a higher cost of living.

Novo Nordisk AS engages in the research, development, manufacture, and marketing of pharmaceutical products. It operates through the Diabetes and Obesity Care; and Biopharmaceuticals segments. The Diabetes and Obesity Care segment covers insulins, glucagon-like-peptide 1, other protein-related products, oral anti-diabetic drugs and obesity. The Biopharmaceuticals segment handles the research, development, manufacture, and distribution of products within the areas of haemophilia, growth hormone, hormone replacement, inflammation and other therapy areas.